4-Methoxybenzenesulfonyl chloride → N1-(cyclopentyloxy)-4-methoxy-1-benzenesulfonamide

HRID 29152Notes

Reaction equation

HRID 29152 reaction equation
[CH:1]1([O:6][N:7]2C(=O)C3C(=CC=CC=3)C2=O)[CH2:5][CH2:4][CH2:3][CH2:2]1.NN.[CH3:20][O:21][C:22]1[CH:27]=[CH:26][C:25]([S:28](Cl)(=[O:30])=[O:29])=[CH:24][CH:23]=1.C(N(CC)C(C)C)(C)C>O1CCCC1>[CH:1]1([O:6][NH:7][S:28]([C:25]2[CH:24]=[CH:23][C:22]([O:21][CH3:20])=[CH:27][CH:26]=2)(=[O:30])=[O:29])[CH2:2][CH2:3][CH2:4][CH2:5]1

Participants

6

Procedure

A mixture of 2-(cyclopentyloxy)-1H-isoindole-1,3(2H)-dione (3.00 g, 12.99 mmol) in anhydrous tetrahydrofuran (15 mL) at ambient temperature under an Argon atmosphere was treated with anhydrous hydrazine (0.448 mL, 14.29 mmol). After stirring vigorously for 1.5 hours, the resulting slurry was filtered and washed with approximately 15 mL of anhydrous tetrahydrofuran. The filtrate was combined with 4-methoxybenzenesulphonyl chloride (2.95 g, 14.29 mmol) and N,N-diisopropylethylamine (2.72 mL, 15.6 mmol). After stirring at ambient temperature for approximately 18 hours, the reaction mixture was evaporated in vacuo to a residue and partitioned between ethyl acetate and 1N hydrochloric acid. The layers were separated and the organic phase was extracted again with ethyl acetate. The combined organic layers were washed with 5% w/v potassium carbonate and brine, dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to a residue. The crude material was purified on flash grade silica gel eluting with 15:85 ethyl acetate:hexane. Fractions containing the product were combined, evaporated in vacuo, and dried under high vacuum to provide N1-(cyclopentyloxy)-4-methoxy-1-benzenesulfonamide (2.771 g, 79%) as an oil. H1-NMR (chloroform-D3): 1.61 (m, 8H), 3.87 (s, 3H), 4.57 (m, 1H), 6.67 (s, 1H), 6.99 (m, 2H), 7.83 (m, 2H). MS(ESI): 294 (M+Na).

Workup

  1. filtrationthe resulting slurry was filtered
  2. washwashed with approximately 15 mL of anhydrous tetrahydrofuran
  3. stirringAfter stirring at ambient temperature for approximately 18 hours
  4. customthe reaction mixture was evaporated in vacuo to a residue
  5. custompartitioned between ethyl acetate and 1N hydrochloric acid
  6. customThe layers were separated
  7. extractionthe organic phase was extracted again with ethyl acetate
  8. washThe combined organic layers were washed with 5% w/v potassium carbonate and brine
  9. dry with materialdried over anhydrous magnesium sulfate
  10. filtrationfiltered
  11. customevaporated in vacuo to a residue
  12. customThe crude material was purified on flash grade silica gel eluting with 15:85 ethyl acetate
  13. additionFractions containing the product
  14. customevaporated in vacuo
  15. customdried under high vacuum

Sources & evidence

ORD record
ord-8b94249bf3b54c4d96feff48a913121f
Source dataset
uspto-grants-2008_09
Patent number
US07419967B2

Reaction notes

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